BACKGROUND OF THE INVENTION
1. Fields of the Invention
[0001] This invention relates to a water based ink capable of decolorizing or discoloring
written or printed letters or images through an organic solvent or heating, which
is used for a writing instrument such as roller ball, marker, etc., printing ink,
ink jet.
2. Description of the Prior Art
[0002] Lately, as an ink capable of decolorizing or discoloring, there have been developed
and have practically been used an ink of aqueous dye type utilizing an oxidation and
reduction reaction (JP-B-54-22344) and an ink of oily dye type using leuco dyes (JP-B-2-29102).
Since the above described ink is an ink of dye type, however, written lines thereof
are inferior in water proof property and light proof property and when writing on
a paper, there occur blurring or bleeding through it. Furthermore, in the case of
an ink of the type utilizing an oxidation and reduction reaction, such a problem arises
that writing cannot again be carried out because a decolorizing solution containing
a reducing agent is excessively coated during decolorizing and the reducing agent
remains on a decolorized site. As a prior art technique, an ink capable of decolorizing
by irradiation of infrared rays, has been known (JP-A-6-73319), but this ink meets
with a problem that the ink or written lines tend to fade.
[0003] As a method for solving the above described problem, it can be considered to use
a pigment for a colorant. In general, an ink using a pigment is excellent in water
proof property as well as light proof property of written lines, so that the blurring
or bleeding through is hard to occur, as well known in the art. As a method of pigmentizing
using a leuco dye, there are proposals to make pigments by applying methods for preparing
tonors to be used for printers or copiers (JP-A-10-88046, JP-A-10-287081). In order
to decolorize written lines of the ink, based on JP-A-10-287081, the paper for writing
is immersed in a special remover, followed by heating, and the decolorizing is thus
rendered possible. This teaches that it is impossible to readily effect the decolorizing.
The ink based on JP-A-10-88046 comprises a leuco dye, developer, decolorizer and resin,
in which the leuco dye and developer are interacted and are in color-developed state.
This decolorizer is a material having such a property as preferentially combining
with the developer during melting the resin or dissolving the resin with a solvent,
whereby the decolorizing is rendered possible with an organic solvent and/or by heating.
[0004] In addition, as an ink for a writing instrument to which the above described technique
is applied, a water based ink composition for a roller ball has been proposed (Japanese
Patent Application No. 249544/2000). The above described pigment has an advantage
that repeated writing can be carried out on a decolorized site, since a leuco dye
and decolorizer are coated with a resin and are not brought into direct contact with
each other.
[0005] However, the above described colorant is generally prepared by mixing and kneading
a color former, developer, decolorizer and resin to obtain a lump of product and then
pulverizing in gaseous phase by means of a jet mill to give the colorant. The colorant
prepared by the above described method has the following disadvantages that:
1) it is difficult to obtain a colorant with a particle or grain diameter of at most
3 µ m in view of the structure of a pulverizer, during which an ink prepared therefrom
meets with problems on the precipitation and adhesiveness property of the colorant,
2) the grain diameter is not uniform, so writing feel is bad,
3) the surface of the colorant is not smooth, so diffused reflection of light takes
place to cause white turbidity seen as pale color,
4) since there is a color-developing component even in the inside of the colorant,
not related with the color tone of the ink, the color-developing component is present
in an amount than required,
5) because of the above described items 3) and 4), the ratio of the color-developing
component is increased, resulting in increase of the cost and
6) since the decolorizer is also contained in the colorant, the resultant water based
ink encounters a problem of fading of the ink color during passage of time.
[0006] The prior art ink of a dye type, capable of decolorizing or discoloring, is inferior
in water proof property and light proof property and when writing on a paper, there
occurs blurring or bleeding of the ink through the paper. Moreover, such a problem
arises that writing cannot again be carried out where the decolorizing has been carried
out. In the case of an ink of a pigment type, there is also a problem that fine granulation
is difficult, writing feel is bad and color tone is too pale.
SUMMARY OF THE INVENTION
[0007] It is an object of the present invention to provide an ink having a uniform and fine
grain diameter, deep color tone and no problem of fading, which is prepared by another
method than that of pulverizing a pigment capable of decolorizing or discoloring in
gaseous phase.
[0008] It is another object of the present invention to provide a process for the production
of an ink having a uniform and fine grain diameter, comprising adding a coloring material
such as leuco dyes, etc. and developer to a suspension of spherical fine grains consisting
of at least one member selected from polyolefins and other polymers containing, as
a constitutional unit, at least one monomer selected from the group consisting of
acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl acrylate and methyl
methacrylate.
[0009] These objects can be achieved by a water based ink comprising a colorant consisting
of spherical fine grains colored by a color former, the said spherical fine grains
consisting of at least one member selected from polyolefins and other polymers containing,
as a constitutional unit, at least one monomer selected from the group consisting
of acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl acrylate and methyl
methacrylate.
DETAILED DESCRIPTION OF THE INVENTION
[0010] The inventors have found that when an ink is prepared by coloring spherical fine
grains obtained by a polymerization reaction with a color former such as leuco dyes,
not by pulverizing a lump of product, for example, using a jet mill for the preparation
of a pigment used in the ink, decolorizing or discoloring can be effected by an organic
solvent and/or heating, and have reached the present invention. Since the spherical
fine grains herein obtained by emulsion polymerization and/or suspension polymerization
can be formed into substantially true spheres while making uniform the grain diameter
with a high precision upto a mean grain diameter of about 0.05 to 1 µ m, it is posssible
to solve the problems as an ink for a writing instrument that the grain diameter is
large or the grain diameter is not uniform. Moreover, the dye adheres to the surface
of the grain, so that the color tone of the colorant is deep, the quantity of the
dye to be used is saved and the colorant can be prepared with a lower cost.
[0011] The prior art ink to be decolorized has been rendered capable of decolorizing by
tracing a decolorizing liquid containing a decolorizer after writing or previously
incorporating a decolorizer in an ink. In the present invention, on the other hand,
decolorizing or discoloring is made possible by using an organic solvent and/or heating
without separately tracing a decolorizer liquid containing a decolorizer or adding
a decolorizer to an ink, based on finding that general papers have a decolorizing
effect for the present ink. However, when writing or printing is carried out on an
acidic paper having a developing action or a glass or plastic having no decolorizing
action, are sometimes not sufficiently decolorized or discolored only by an organic
solvent and/or heating. In such a case, decolorizing or discoloring is made possible
by incorporating a basic compound such as aqueous ammonia or triethanolamine in an
organic solvent. As in the prior art, decolorizing or discoloring can be carried out
by an organic solvent and/or heating by adding to an ink a decolorizer which does
not react with colored spherical fine grains, nor fades the ink color. For example,
Lewis basic materials such as polyvinylpyrrolidone, urea, ethyleneurea, hydantoin
and the like can be used.
[0012] That is, the present invention and embodiments thereof can be summarized below:
(1) A water based ink comprising a colorant consisting of spherical fine grains colored
by a color former, the said spherical fine grains consisting - of at least one member
selected from resins.
(2) The water based ink as described in the foregoing (1), wherein the colorant consists
of spherical fine grains colored by a color former, the said spherical fine grains
consisting of at least one member selected from polyolefins and other polymers containing,
as a constitutional unit, at least one monomer selected from the group consisting
of acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl acrylate and methyl
methacrylate.
(3) The water based ink as described in the foregoing (1) or (2), wherein the colorant
is contained in a proportion of 5 to 40 weight %.
(4) The water based ink as described in any one of the foregoing (1) to (3), wherein
the color former is a leuco dye.
(5) The water based ink as described in any one of the foregoing (1) to (4), wherein
the spherical fine grains are colored with a leuco dye to obtain a colored ink.
(6) The water based ink as described in any one of the foregoing (1) to (5), wherein
decolorizing or discoloring is carried out by at least one of using an organic solvent
and heating.
(7) The water based ink as described in any one of the foregoing (1) to (6), wherein
the developer for color-developing a leuco dye is at least one compound selected from
the group consisting of phenolic hydroxyl group-containing compounds and phosphate
group-containing compounds.
(8) The water based ink as described in any one of the foregoing (1) to (7), wherein
the ink is acidic.
(9) The water based ink for a writing instrument, wherein the spherical fine grains
used in the ink described in any one of the foregoing (1) to (8) have a mean grain
diameter of at most 1 µ m.
(10) A process for the production of a water-based ink, comprising adding at least
one member selected from the group consisting of organic solvents and surfactants
to a color former and developer to color-develop a dye solution and dropwise adding
the thus color-developed dye solution to a suspension of spherical fine grains consisting
of at least one member selected from polyolefins and other polymers containing, as
a constitutional unit, at least one monomer selected from the group consisting of
acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl acrylate and methyl
methacrylate, thereby coloring the spherical fine grains.
PREFERRED EMBODIMENTS OF THE INVENTION
[0013] In the present invention, an ink capable of decolorizing and discoloring by using
an organic solvent and/or heating is obtained by coloring spherical fine grains consisting
of at least one member selected from resins, in particular, polyolefins and other
polymers containing, as a constitutional unit, at least one monomer selected from
the group consisting of acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl
acrylate and methyl methacrylate with a color former, in particular, a leuco dye color-developed
by the use of a developer, thus resulting in a water based ink.
[0014] The color former used in the present invention typically includes leuco dyes, for
example, compounds having lactone ring in the molecule, such as triphenylmethane type,
diphenylmethane type, spiropyran type, fluoran type, rhodamine lactam type, etc. One
or more of these compounds can be used in admixture.
[0015] Examples of these compounds are "CVL", "Green DCF", "Vermilion DCF", "Red DCF", "Orange
DCF", "TH-106", "TH-107", "TH-108", "TH-109", "CF-51" and "D. L. M. B.", all of which
are commercial names of Hodogaya Chemical Co., Ltd., "DEBN", "RED 500", "RED 520",
"S-205", "Black 100", "Black 202", "Black 305", "ETAC", "Blue 220", "NIR Black 78",
"Green 300" and "PINK 535", all of which are commercial names of Yamada Chemical Co.,
Ltd. and "ODB", "ODB-2", "ODB-7", "Black-15", "Black-173", "Blue-63", "Blue-502",
"Green-40", "Red-3", "Red-40", "MNSP", "LCV", "GN-2", "GN-169" and "GN-118", all of
which are commercial names of Yamamoto Chemical, Inc.
[0016] As the developer capable of coloring the color former through formation of a pair
thereof, there are used compounds having phenolic hydroxyl group in the molecule,
such as hydroxyacetophenone type, hydroxybenzophenone, gallic acid estyer type, benzenetriol
type, bisphenol type, triphenol type, cresol type compounds, etc., or compounds having
phosphate group in the molecule, such as phosphoric acid, phosphoric acid monoesters,
phosphoric acid diesters, etc., individually or in combination.
[0017] Examples of these compounds are, as the compounds having phenolic hydroxyl group,
dihydroxyacetophenone, trihydroxyacetophenone, dihydroxybenzophenone, trihydroxybenzophenone,
tetrahydroxybenzophenone, dihydrobenzoic acid, bisphenol, hydroxyphenylalkyl-benzotriazole,
methylenetris-p-cresol, gallic acid alkylesters, etc., and as the compounds having
phosphate group, monoalkylphosphoric acid esters, dialkylphosphoric acid esters, polyoxyethylene
mono-alkylphosphoric acid esters, polyoxyethylene dialkylphosphoric acid esters, etc.,
the alkyl group being selected from methyl, ethyl, propyl, butyl, nonyl, lauryl, oleyl
and stearyl groups. Commercial names of the compounds having phosphate group are Phosphanol
Series (Toho Chemical Industry Co., Ltd.), Plysurf Series (Dai-ichi Kogyo Seiyaku
Co., Ltd.), Newkol 565-PS (Nippon Nyukazai Co., Ltd.), etc.
[0018] In the present invention, there can be used a leuco dye in a proportion of 0.1 to
2 weight % and a developer in a proportion of 0.1 to 3 weight % to the weight of the
ink. The proportion of the developer to the leuco dye, depending on the valence of
the developer, is generally at least 1 chemical equivalent, preferably 1 to 3 chemical
equivalent. Furthermore, the colored spherical fine grains can be used in a proportion
of 5 to 40 weight %, preferably 10 to 25 weight % to the weight of the ink. The proportion
of the solvent used in the above described ink is 5 to 30 weight % in the case of
using the colored spherical fine grains as a suspension for the preparation of an
ink, and 0 to 10 weight % in the case of meaning an organic solvent (and/or surfactant)
used for coloring the spherical fine grains.
[0019] As an acid for acidifying the ink, there can be used inorganic acids such as hydrochloric
acid, nitric acid, sulfuric acid, phosphoric acid, thiosulfuric acid, chloric acid,
chlorous acid, perchloric acid, etc., or organic acids such as formic acid, acetic
acid, propionic acid, citric acid, malic acid, oxalic acid, phenol, cresol, acrylic
acid, methacrylic acid, etc. From the standpoint of safety for the human body, it
is preferable to choose acetic acid, hydrochloric acid, citric acid, malic acid and
the like. Since the developer, namely, the compounds having phenolic hydroxyl group
or compounds having phosphate group functions also as an acidifying material, moreover,
the ink can be acidified without using the above described acidifying material depending
on the property or use object of the ink.
[0020] The spherical fine grains consist of at least one of polyolefins and other polymers
containing, as a constitutional unit, at least one monomer selected from the group
consisting of acrylonitrile, styrene, acrylic acid, methacrylic acid, methyl acrylate
and methyl methacrylate, in the form of homopolymers or copolymers. Above all, acrylonitrile-styrene-methacrylic
acid copolymers, methyl methacrylate polymer or polyethylene are preferably used.
For the polymerization, any one of emulsion polymerization, suspension polymerization
and vapor phase polymerization can be applied. During the same time, the mean grain
diameter of the spherical fine grains is not particularly limited in the case of a
printing ink, but can be allowed upto 0.05 to 1 µ m, more preferably 0.05 to 0.5 µ
m, in the case of an ink for a writing instrument. When the average grain diameter
of the spherical fine grains is smaller than 0.05 µ m, it is not considered that problems
arise on practical use, but in fact, preparation thereof is very difficult. When it
exceeds 1 µ m, such a problem takes place that the ink is hard to pass through a nib
and settling of the colorant occurs in the ink, thus resulting in difficulty of writing.
[0021] In addition, as a fixing resin for allowing the colorant to adhere to a paper surface,
a water-soluble resin or aqueous resin emulsion can be used. As the water-soluble
resin, there can be used water-soluble nylon resin, water-soluble polyvinylacetal
resin, water-soluble acrylic resin, water-soluble polyamide resin, polyethylene oxide,
polyvinyl alcohol, polyvinylpyrrolidone, esterified starch, dextrin, reducing malt
sugar, sugar alcohol, carboxymethyl cellulose, etc. Polyvinyl alcohol, polyvinylpyrrolidone
and dextrin are preferably used. As the aqueous resin emulsion, there can be used
ethylene-vinyl acetate emulsion, ethylene-vinyl acetate-vinyl chloride emulsion, ethylene-vinyl
acetate acrylic emulsion, acrylic emulsion, styrene acrylic emulsion, styrene acrylonitrile
emulsion, acrylonitrile butadiene emulsion, acrylic butadiene emulsion, urethane emulsion,
polyester emulsion, etc. Ethylene-vinyl acetate emulsion and ethylene-vinyl acetate-vinyl
chloride emulsion are preferably used. These materials can be used individually or
in combination.
[0022] When, for the purpose of discoloring, ordinary known dyes and/or pigments are simultaneously
used in addition to the colorant capable of decolorizing, only the color of the color
former is decolorized to retain the color of only the ordinary known dyes and/or pigments,
thus rendering possible the discoloring. As the dye, there can be used acid dyes,
basic dyes and direct dyes. As the pigment, there can be used organic pigments such
as those of azo type, phthalocyanine type, quinacridone type, anthraquinone type,
dioxazine type, etc., inorganic pigments such as those of carbon black, synthetic
mica, titanium dioxide, metallic fine powder, etc. and known resin pigments, obtained
by coloring spherical fine grains obtained by emulsion polymerization with ordinary
dyes, individually or in combination. Preparation of the ink capable of being discolored
is generally carried out by coloring spherical fine grains obtained by emulsion polymerization
through joint use of a color former and ordinary dye, whereby only the color of the
color former is decolorized to retain the color of only the ordinary known dyes, thus
rendering possible the discoloring.
[0023] As the organic solvent for a solvent for decolorizing, there are used ketone type
solvents such as acetone, methyl ethyl ketone, methyl propyl ketone, diethyl ketone,
ethyl propyl ketone, dipropyl ketone, acetyl acetone, acetophenone, 3-methyl-2-batanone,
3,3-dimethyl-2-butanone, 2,4-dimethyl-3-pentanone, 2,6-dimethyl-4-heptanone, etc.,
ether type solvents such as dimethyl ether, diethyl ether, methyl ethyl ether, dipropyl
ether, dibutyl ether, 1,2-dimethoxyethane, 1,2-diethoxyethane, pyrane, furan, methylfuran,
tetrahydrofuran, ethylene oxide, propylene oxide, dioxane, etc., ester type solvents
such as ethyl acetate, butyl acetate, isoamyl acetate, methyl acrylate, ethyl acrylate,
methyl methacrylate, ethyl methacrylate, etc., alcohol type solvents such as methanol,
ethanol, propanol, butanol, pentanol, hexanol, benzyl alcohol, ethylene glycol, propylene
glycol, etc., glycol ether type solvents such as 2-methoxyethanol, 2-ethoxyethanol,
1-methoxy-2-propanol, etc., glycol ether ester type solvents such as methylglycol
acetate, ethylglycol acetate, etc., hydrocarbon type solvents such as hexane, heptane,
cyclohexane, methylcyclohexane, etc., aromatic hydrocarbon solvents such as benzene,
toluene, xylene, etc., halogenated hydrocarbon type solvents such as methyl chloride,
methylene chloride, chloroform, dichloroethane, trichloroethane, tetrachloroethane,
perchloroethane, perchloroethyelene, chlorobenzene, etc., hetero atom-containing hydrocarbon
type solvents such as aniline, toluidine, pyridine, bipyridine, dimethylimidazolidinone,
dimethyl sulfoxide, etc., individually or in combination. From the standpoint of safety
for the human body and drying property, etc. of the solvents, in particular, acetone,
1,2-dimethoxyethane and 1,2-diethoxyethane are preferable. The hetero atom herein
referred means, in particular, nitrogen atom and sulfur atom, not including oxygen
atom.
[0024] A solvent composition for decolorizing, comprising a decolorizing assistant for promoting
decolorizing in addition to a solvent for decolorizing, can be used as a solvent for
decolorizing. As the decolorizing assistant, there can be used basic compounds, for
example, inorganic basic compounds such as alkali metal hydroxides or alkaline earth
metal hydroxides each having basic hydroxyl group, alkali metal carbonates or alkaline
earth metal carbonates, alkali metal alkoxides and the like, and Lewis basic compounds
such as ammonia, urea and urea derivatives, primary amines, secondary amines, tertiary
amines, primary amides, secondary amides and tertiary amides, individually or in combination.
When decolorizing is carried out using a solvent composition for decolorizing, containing
the above described basic compound, a written line or image can be decolorized. When
the basic compound used herein has no volatility, however, the basic compound remains
on a site where the solvent composition for decolorizing has been used and rewriting
or reprinting cannot be effected on this site since the ink instantaneously is reacted
with the basic compound and decolorized. When the basic compound has a volatility,
on the other hand, the basic compound vaporizes from a site where the solvent composition
for decolorizing has been used and rewriting or reprinting can be carried out thereon.
As a volatile basic compound for the solvent composition for decolorizing, there can
be used, individually or in combination, amines such as monoethylamine, diethylamine,
triethylamine, dipropylamine, butylamine, allylamine, ethylenediamine, monoethanolamine,
diethanolamine, triethanolamine, propanolamine, aniline, pyridine, bipyridine, 3,5-dimethylimidazolidinone,
etc. and amides such as formamide, dimethylformadmide, etc. Triethanolamine is more
preferably used from the standpoint of decolorizing capacity, safety for the human
body, drying property of the solvent.
[0025] If necessary, the commonly used additives, for example, surfactants, preservatives,
rust preventives, water-miscible humectants, lubricants, dispersing resins, etc. can
be added to the ink within the scope of the present invention, which should not, of
course, hinder the decolorizing and/or discoloring through reaction with the coloring
materials, developers and spherical fine grains.
Example
[0026] The following examples are given in order to illustrate the invention in more detail
without limiting the same.
(Example 1)
[0027] An apparatus comprising a four neck flask of 2 litters, condenser, thermometer, 500
ml separating funnel for charging monomers and stirring means was set in a thermostat
vessel and 300 g of ion exchanged water was charged in the flask, followed by heating
to 80 °C.
[0028] A monomer mixture of 140 g of acrylonitrile, 228 g of styrene and 32 g of methacrylic
acid was added to a mixed solution of 218 g of ion exchanged water and 80 g of sodium
polyoxyethylene alkyl ether sulfate, mixed and stirred, in which 2 g of ammonium persulfate
was then dissolved, and the resulting mixture was dropwise added from the above described
separating funnel to the flask for 3 hours and polymerization was finished after further
5 hours.
[0029] 20 g of ion exchanged water and 16 g of glycerine were then added with stirring to
50 g of the resulting suspension of the emulsified polymer to prepare a suspension.
On the other hand, a dye solution was prepared by adding 2 g of acetone to 0.6 g of
CVL (blue type leuco dye, manufactured by Hodogaya Chemical Co., Ltd., commercial
name) and 1.2 g of propyl gallate (developer, manufactured by Wako Pure Chemical Industries,
Ltd.) with heating and color-developing to evaporate the acetone, and further adding
2 g of PELEX NBL (surfactant, sodium alkylnaphthalenesulfonate, manufactured by Kao
Corporation) with heating and stirring. The thus prepared dye solution was dropwise
added to the foregoing suspension and the resulting suspension was heated at 50 °C
and dyed for 1 hour to obtain a blue ink with a mean grain diameter of 0.12 µm and
a pH of 2.5. This ink was charged in a polyethylene reservoir in an analogous manner
to a commercially available reservoir type marker (OPTEX or ZEBRITE, manufactured
by Zebra Co., Ltd., commercial name), loaded in a reservoir and fitted with a polyethylene
nib and cap, thus preparing a blue marker. Using the thus prepared marker, writing
was carried out by hand on a PPC paper (manufactured by Oji Paper Co., Ltd., commercial
name).
(Example 2)
[0030] 30 g of ion exchanged water and 15 g of glycerine were added to 50 g of an emulsified
polymer suspension obtained in Example 1 to form a solution. On the other hand, 3.0
g of ethylene glycol and 2.0 g of PELEX NBL were added to 0.4 g of RED 40 (red type
leuco dye, manufactured by Yamamoto Chemical, Inc., commercial name) and 2.0 g of
Phosphanol RM 710 (developer, mixture of phosphoric acid monoalkyl ester and phosphoric
acid dialkyl ester, manufactured by Toho Chemical Industry Co., Ltd., commercial name),
heated, stirred and color-developed to form a dye solution which was then dropwise
added to the foregoing solution. The resulting suspension was then heated and dyed
at 50 °C for 1 hour to obtain a red ink with a mean grain diameter of 0.12 µ m. To
30 g of the resulting ink was added 0.1 g of Kayarus Turquoise Blue GL (blue dye,
manufactured by Nippon Kayaku Co., Ltd., commercial name) to obtain a violet ink having
a pH of 3.1. The resulting ink was charged in an ink tank in an analogous manner to
a commercially available liquid ink system marker (SPARKY 1 or ZAZZLE BRIGHTS, manufactured
by Zebra Co., Ltd., commercial name), loaded by a bulb-charged end cover and fitted
with a polyester nib and cap, thus preparing a violet marker. Using the thus prepared
marker, writing was carried out by hand on a PPC paper (manufactured by Oji Paper
Co., Ltd., commercial name).
(Example 3)
[0031] 100 g of ion exchanged water, 3 g of PELEX NBL and 20 g of MP-1451 (methyl methacrylate
emulsified polymer, manufactured by Soken Chemical & Engineering Co., Ltd., commercial
name) were added to a vessel containing 75 g of glass beads (2 mm), covered and shaken
for 5 minutes by means of a shaker to disperse spherical fine grains. To 50 g of the
resulting dispersed suspension was dropwise added with stirring a solution obtained
by adding 0.3 g of PINK 535 (pink type leuco dye, manufactured by Yamada Chemical
Co., Ltd., commercial name) and 1 g of di-n-butyl phosphate (developer, manufactured
by Tokyo Kasei Kogyo Co., Ltd.) to 2 g of ethyl alcohol and 2 g of ethylene glycol,
dissolving, heating and color-developing, and then heated and dyed at 50 °C for 1
hour to obtain a pink ink with a mean grain diameter of 0.15 µm and a pH of 4.4. The
resulting ink was charged in an ink tank as an ink for an ink jet printer using a
piezo element (PM-700J, manufactured by Seiko Epson Corporation, commercial name)
to prepare an ink cartridge for an ink jet printer. Using the thus prepared ink cartridge,
printing was carried out on an ink-jet print paper (manufactured by Victor Company
of Japan, Ltd., commercial name).
(Example 4)
[0032] 20 g of the ink obtained in Example 3 and 10 g of LUMIKOL NKW-3005 (aqueous dispersion
of fluorescent resin pigment, manufactured by Nippon Keiko Kagaku Co., Ltd., commercial
name) were mixed with stirring to obtain an orange ink. The resulting ink showed a
pH of 5.8. The resulting ink was charged in an ink tank as an ink for an ink jet printer
using a piezo element (PM-700J, manufactured by Seiko Epson Corporation, commercial
name) to prepare an ink cartridge for an ink jet printer. Using the thus prepared
ink cartridge, printing was carried out on an ink-jet print paper (manufactured by
Victor Company of Japan, Ltd, commercial name).
(Example 5)
[0033] 50 g of ion exchanged water, 2 g of PELEX NBL and 10 g of MP-300F (methyl methacrylate
emulsified polymer, manufactured by Soken Chemical & Engineering Co., Ltd., commercial
name) were added to a vessel containing 50 g of glass beads (2 mm), covered and shaken
for 5 minutes by means of a shaker to disperse spherical fine grains. To the resulting
dispersed suspension was dropwise added with stirring a solution obtained by adding
0.3 g of RED DCF and 2 g of Newcol-565-PS (developer, polyoxyethylenenonylphenylether
phosphoric acid ester, manufactured by Nippon Nyukazai Co., Ltd., commercial name)
to 2 g of ethylene glycol and 1.5 g of PELEX NBL, dissolving, heating and color-developing,
and then heated and dyed at 50 °C for 1 hour to obtain a red ink with a mean grain
diameter of 0.35 µ m. To 30 g of the resulting ink was added 0.15 g of xanthane gum
with stirring to obtain an ink for a gel ink roller ball having a pH of 4.6. The resulting
ink for a gel ink roller ball was charged in a polypropylene tube in an analogous
manner to a commercially available gel ink roller ball (BW-100, manufactured by Zebra
Co., Ltd., commercial name, stainless tip ball diameter 0.7 mm). Then the tube was
fitted with a pen point, charged with a suitable quantity of an ink follower from
the end thereof and subjected to defoaming at 200 G by a separater to prepare a roller
ball. Using the the thus prepared roller ball, writing was carried out by hand on
a PPC paper (manufactured by Oji Paper Co., Ltd, commercial name).
(Example 6)
[0034] 50 g of Chemipearl W-700 (polyolefin vapor phase polymer dispersion, manufactured
by Mitsui Sekiyu Kagaku Kogyo Co., Ltd., commercial name), 20 g of ion exchanged water,
10 g of ethylenen glycol and 10 g of glycerine were added to a beaker and stirred
to obtain a dispersion. To the resulting dispersion was dropwise added with stirring
a solution obtained by adding 0.3 g of PINK 535, 1 g of di-n-butyl phosphate and 0.1
g of Fast Green FCF (green type dye, manufactured by Daiwa Dyestuff Mfg. Co., Ltd.,
commercial name) to 2 g of ethyl alcohol and 2 g of ethylene glycol, dissolving, heating
and color-developing, and then heated and dyed at 65 °C for 1 hour to obtain a black
ink with a mean grain diameter of 1 µ m. To 30 g of the resulting ink was added 0.6
g of PVA-124 (polyvinyl alcohol, manufactured by Kuraray Co., Ltd., commercial name),
mixed and stirred to prepare an ink for printing, having a pH of 5.8. Using the thus
prepared ink, printing was carried out on a PPC paper (manufactured by Oji Paper Co.,
Ltd., commercial name) by means of an ordinary relief printing machine. -
(Comparative Example 1)
[0035] Ion exchanged water was used in place of the emulsified polymer of Example 1 to prepare
an aqueous solution of a blue dye. The resulting ink had a pH of 4.0. The resulting
ink was charged in an ink tank in an analogous manner to a commercially available
liquid ink system marker (SPARKY 1 or ZAZZLE BRIGHTS, manufactured by Zebra Co., Ltd.,
commercial name), loaded by a bulb-charged end cover and fitted with a polyester nib
and cap, thus preparing a blue marker. Using the thus prepared marker, writing was
carried out by hand on a PPC paper (manufactured by Oji Paper Co., Ltd., commercial
name).
(Comparative Example 2)
[0036] 0.1 g of Rhodamine B was used in place of CVL of Example 1 to prepare a pink ink.
The resulting ink had a pH of 3.0. The resulting ink was charged in an ink tank in
an analogous manner to a commercially available liquid ink system marker (SPARKY 1
or ZAZZLE BRIGHTS, manufactured by Zebra Co., Ltd., commercial name), loaded by a
bulb-charged end cover and fitted with a polyester nib and cap, thus preparing a pink
marker. Using the thus prepared marker, writing was carried out by hand on a PPC paper
(manufactured by Oji Paper Co., Ltd., commercial name).
(Comparative Example 3)
[0037] The violet ink obtained in Example 2 was treated with aqueous ammonia to adjust pH
to 8.5 and obtain a blue ink. The resulting ink was charged in an ink tank in an analogous
manner to a commercially available liquid ink system marker (SPARKY 1 or ZAZZLE BRIGHTS,
manufactured by Zebra Co., Ltd., commercial name), loaded by a bulb-charged end cover
and fitted with a polyester nib and cap, thus preparing a blue marker. Using the thus
prepared marker, writing was carried out by hand on a PPC paper (manufactured by Oji
Paper Co., Ltd., commercial name).
(Comparative Example 4)
[0038] 100 g of ion exchanged water, 2 g of SANMORIN 0T-70 (sodium dioctylsulfosuccinate,
surfactant, manufactured by Sanyo Kasei Kogyo Co., Ltd., commercial name) and 25 g
of MX-300 (methyl methacrylate emulsified polymer, manufactured by Soken Chemical
& Engineering Co., Ltd., commercial name) were added to a vessel containing 60 g of
glass beads (2 mm), covered and shaken for 5 minutes by means of a shaker to disperse
spherical fine grains. To 50 g of the resulting dispersed suspension was dropwise
added with stirring a solution obtained by adding 0.3 g of PINK 535 and 0.6 g of propyl
gallate to 2 g of ethyl alcohol, dissolving, heating and color-developing, and then
heated and dyed at 50 °C for 1 hour to obtain a pink ink with a mean grain diameter
of 3 µ m and a pH-of 6.3. The resulting ink was charged in an ink tank in an analogous
manner to a commercially available liquid ink system marker (SPARKY 1 or ZAZZLE BRIGHTS,
manufactured by Zebra Co., Ltd., commercial name), loaded by a bulb-charged end cover
and fitted with a polyester nib and cap, thus preparing a pink marker. Using the thus
prepared marker, writing was carried out by hand on a PPC paper (manufactured by Oji
Paper Co., Ltd., commercial name).
(Test Method)
[0039] Test papers obtained by writing or printing in the foregoing Examples 1 to 6 and
Comparative Examples 1 to 4 were used as test samples and subjected to the following
test:
Estimation of Ink Color
[0040] The color of the resulting ink was visually confirmed.
Estimation of Color of Written or Printed Line on Test Paper
[0041] The color of the written or printed line on a test paper in each of Examples and
Comparative Examples was visually confirmed.
Estimation of Decolorizing or Discoloring by Solvent for Decolorizing
[0042] Several drops of acetone as a solvent for decolorizing were dropwise added to the
written or printed line on a test paper in each of Examples and Comparative Examples
and after drying, the color of the written or printed line was visually confirmed.
Estimation of Decolorizing or Discoloring by Heating for Decolorizing
[0043] An iron heated at about 200 °C was pressed against the written or printed line in
each of Examples and Comparative Examples and after cooling, the color of the written
or printed line was visually confirmed.
(Test Results)
[0044] Test results are shown in Table 1.
Table 1 -
Example No. |
Estimation of Color of Ink |
Estimation of Color of Written or Printed Line on Test Paper |
Estimation of Decolorizing or Discoloring by Organic Solvent |
Estimation of Decolorizing or Discoloring by Heating |
1 |
blue |
blue |
colorless |
colorless |
2 |
violet |
violet |
blue |
blue |
3 |
pink |
pink |
colorless |
colorless |
4 |
orange |
orange |
yellow |
yellow |
5 |
red |
red |
colorless |
colorless |
6 |
black |
black |
green |
green |
Comparative Example |
1 |
blue |
colorless |
- |
- |
2 |
pink |
pink |
pink |
pink |
3 |
blue |
blue |
blue |
blue |
4 |
pink |
- |
- |
- |
(note) "-" No test was carried out. |
[0045] In the case of Comparative Example 1, in which the spherical fine grains were not
dyed, when writing on the paper, the color former reacted with the paper having a
decolorizing function and the written line was not obtained. In Comparative Example
2, in which dyeing was carried out by the ordinary dye, decolorizing or discoloring
was impossible. In Comparative Example 3, in which the ink was basic, the coloring
material functioned as a decolorizer in the ink and was in decolorized state, so the
color of the ink was only blue corresponding to the ordinary dye, which taught that
decolorizing could not be carried out. In Comparative Example 4, in which the spherical
fine grains with a relatively larger grain diameter were used, the ink could not be
passed through the wadded fiber point of the marker, i.e. writing was impossible.
[0046] In the case of Examples 1 to 6 according to the present invention, on the other hand,
decolorizing or discoloring was favorably accomplished by using organic solvents and/or
heating, whereby the effects of the present invention were clearly proved.
Advantages of the Invention
[0047] When the specified ink according to the present invention, in particular, comprising
a colorant consisting of spherical fine grains colored by a coloring material, the
said spherical fine grains consisting of at least one member selected from polyolefins
and other polymers containing, as a constitutional unit, at least one monomer selected
from the group consisting of acrylonitrile, styrene, acrylic acid, methacrylic acid,
methyl acrylate and methyl methacrylate was used, decolorizing or discoloring of letters
or images is capable through an organic solvent or heating.